(Q37258000)

English

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results

scientific article published on 11 June 2009

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

cleft lip with or without cleft palate

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Sandra Daack-Hirsch

object named as

Sandra Daack-Hirsch

9

0 references

Mauricio Arcos-Burgos

object named as

Mauricio Arcos-Burgos

19

0 references

Mary L. Marazita

1

object named as

Mary L Marazita

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Astanand Jugessur

11

object named as

Astanand Jugessur

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Andrew C Lidral

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Jeffrey C Murray

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

L Leigh Field

4

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Brion S Maher

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Toby Goldstein McHenry

6

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Margaret E Cooper

7

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Manika Govil

8

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Bridget Riley

10

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Temis Felix

12

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Lina Morene

13

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

M Adela Mansilla

14

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Alexandre R Vieira

15

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Kim Doheny

16

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Elizabeth Pugh

17

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Consuelo Valencia-Ramirez

18

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

publication date

11 June 2009

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

68

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

151-170

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Dental anomalies as part of the cleft spectrum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Unraveling human cleft lip and palate research

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

CRISPLD2: a novel NSCLP candidate gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Human genetic factors in nonsyndromic cleft lip and palate: an update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Association between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

A mutation in RYK is a genetic factor for nonsyndromic cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Identifying genomic regions for fine-mapping using genome scan meta-analysis (GSMA) to identify the minimum regions of maximum significance (MRMS) across populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Using linkage genome scans to improve power of association in genome scans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Medical sequencing of candidate genes for nonsyndromic cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Progress toward discerning the genetics of cleft lip

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Variation in IRF6 contributes to nonsyndromic cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Significant association between IRF6 820G->A and non-syndromic cleft lip with or without cleft palate in the Thai population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Orofacial clefting: recent insights into a complex trait

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Distinct functions for Bmp signaling in lip and palate fusion in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Gene expression in pharyngeal arch 1 during human embryonic development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Genetic mapping and ENU mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Strong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Identification of SATB2 as the cleft palate gene on 2q32-q33.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Minimal haplotype tagging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Multiplex relative risk and estimation of the number of loci underlying an inherited disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Analysis of the p63 gene in classical EEC syndrome, related syndromes, and non-syndromic orofacial clefts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Power to detect linkage based on multiple sets of data in the presence of locus heterogeneity: comparative evaluation of model-based linkage methods for affected sib pair data.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

A chromosomal duplication map of malformations: regions of suspected haplo- and triplolethality--and tolerance of segmental aneuploidy--in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

A chromosomal deletion map of human malformations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

A mouse model for hereditary thyroid dysgenesis and cleft palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Familial recurrence-pattern analysis of nonsyndromic isolated cleft palate--a Danish Registry study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Nonsyndromic cleft lip with or without cleft palate in west Bengal, India: evidence for an autosomal major locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Pallister-Killian and Fryns syndromes: nosology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Complex segregation analysis of nonsyndromic cleft lip and palate.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Cleft lip with or without cleft palate in Shanghai, China: evidence for an autosomal major locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

6 September 2017

Development of human craniofacial morphology during the late embryonic and early fetal periods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

14 September 2017

Familial recurrence-pattern analysis of cleft lip with or without cleft palate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

14 September 2017

Cleft palate: players, pathways, and pursuits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

28 September 2017

Distribution of the titf2/foxe1 gene product is consistent with an important role in the development of foregut endoderm, palate, and hair.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

28 September 2017

Facial clefting in Tp63 deficient mice results from altered Bmp4, Fgf8 and Shh signaling.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

26 June 2018

Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

26 June 2018

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

26 June 2018

Implementing a unified approach to family-based tests of association.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

26 June 2018

Cleft lip and palate etiology and its meaning in early 20th century England: Galton/Pearson vs. Bateson; polygenically poor protoplasm vs. Mendelism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

26 June 2018

Genetic analysis of cleft lip with or without cleft palate in Danish kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

26 June 2018

Cleft lip with or without cleft palate: reanalysis of a three-generation family study from England

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

26 June 2018

The minimal cleft lip.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

26 June 2018

Temporal and spatial expression of Pax9 and Sonic hedgehog during development of normal mouse palates and cleft palates in TGF-beta3 null embryos.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

A mutation of the p63 gene in non-syndromic cleft lip.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Identification of markers of the midface.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Developmental gene expression profiling of mammalian, fetal orofacial tissue.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Highly parallel SNP genotyping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

TP63 mutation and clefting modifier genes in an EEC syndrome family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

The Rapp-Hodgkin syndrome results from mutations of the TP63 gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Microarray analysis of murine palatogenesis: Temporal expression of genes during normal palate development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Determining trait locus position from multipoint analysis: accuracy and power of three different statistics.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

The family based association test method: strategies for studying general genotype--phenotype associations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Meta-analysis of genome searches

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Analysis of the recurrence patterns for nonsyndromic cleft lip with or without cleft palate in the families of 3,073 Danish probands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

Lods, wrods, and mods: the interpretation of lod scores calculated under different models.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

3 September 2018

A genome wide linkage scan for cleft lip and palate and dental anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2709160

20 October 2018

Genetic analysis of cleft lip with or without cleft palate in Chinese kindreds

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An estimation of the number of susceptibility loci for isolated cleft palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rethinking isolated cleft palate: evidence of occult lip defects in a subset of cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of bone morphogenetic protein 4 gene polymorphisms with nonsyndromic cleft lip with or without cleft palate in Chinese children

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transforming growth factor alpha locus and nonsyndromic cleft lip with or without cleft palate: a reappraisal

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral Asymmetry in Chinese Families with Cleft Lip with or without Cleft Palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FOXE1 gene mutation screening by multiplex PCR/DHPLC in CHARGE syndrome and syndromic and non-syndromic cleft palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Fryns syndrome. Report on 3 new cases]

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interferon regulatory factor 6 (IRF6) is associated with oral-facial cleft in individuals that originate in South America

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three-dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: a possible marker for genetic susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cleft lip with or without cleft palate and dermatoglyphic asymmetry: evaluation of a Chinese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairs

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsyndromic cleft lip with or without cleft palate in China: assessment of candidate regions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lymphedema-distichiasis syndrome and FOXC2 gene mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome‐wide scan for loci predisposing to non‐syndromic cleft lip with or without cleft palate in two large Syrian families

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-scan for loci involved in cleft lip with or without cleft palate in consanguineous families from Turkey

1 reference

https://pubmed.ncbi.nlm.nih.gov/19521098

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1159/000224636

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q37258000&oldid=2219502872"